Discontinuation of β-blocker therapy in stabilised patients after acute myocardial infarction (SMART-DECISION): rationale and design of the randomised controlled trial
- Author(s)
- Ki Hong Choi; Juwon Kim; Danbee Kang; Joon-Hyung Doh; Juhan Kim; Yong Hwan Park; Sung Gyun Ahn; Weon Kim; Jong Pil Park; Sang Min Kim; Byung-Ryul Cho; Chang-Wook Nam; Jang Hyun Cho; Seung-Jae Joo; Jon Suh; Jin-Ok Jeong; Woo Jang; Chang-Hwan Yoon; Jin-Yong Hwang; Seong-Hoon Lim; Sang-Rok Lee; Eun-Seok Shin; Byung Jin Kim; Cheol Woong Yu; Sung-Ho Her; Hyun Kuk Kim; Kyu Tae Park; Jihoon Kim; Taek Kyu Park; Joo-Myung Lee; Juhee Cho; Jeong Hoon Yang; Young Bin Song; Seung Hyuk Choi; Hyeon-Cheol Gwon; Eliseo Guallar; Joo-Yong Hahn
- Keimyung Author(s)
- Nam, Chang Wook
- Department
- Dept. of Internal Medicine (내과학)
- Journal Title
- BMJ Open
- Issued Date
- 2024
- Volume
- 14
- Issue
- 8
- Abstract
- Introduction:
There is a lack of evidence to support the effectiveness of prolonged β-blocker therapy after stabilisation of patients with acute myocardial infarction (AMI) without heart failure (HF) or left ventricular systolic dysfunction.
Methods and analysis:
The SMart Angioplasty Research Team: DEcision on Medical Therapy in Patients with Coronary Artery DIsease or Structural Heart Disease Undergoing InterventiON (SMART-DECISION) trial is a multicentre, prospective, open-label, randomised, non-inferiority trial designed to determine whether discontinuing β-blocker therapy after ≥1 year of maintenance in stabilised patients after AMI is non-inferior to continuing it. Patients eligible for participation are those without HF or left ventricular systolic dysfunction (ejection fraction >40%) who have been continuing β-blocker therapy for ≥1 year after AMI. A total of 2540 patients will be randomised 1:1 to continuation of β-blocker therapy or not. Randomisation will be stratified according to the type of AMI (ie, ST-segment-elevation MI or non-ST-segment-elevation MI), type of β-blocker (carvedilol, bisoprolol, nebivolol or other) and participating centre. The primary study endpoint is a composite of all-cause death, MI and hospitalisation for HF over a median follow-up period of 3.5 years (minimum, 2.5 years; maximum, 4.5 years). Adverse effects related to β-blocker therapy, the occurrence of atrial fibrillation, medical costs and Patient-reported Outcomes Measurement Information system-29 questionnaire responses will also be collected as secondary endpoints.
Ethics and dissemination:
Ethics approval for this study was granted by the Institutional Review Board of Samsung Medical Center (no. 2020-10-176). Informed consent is obtained from every participant before randomisation. The results of this study will be submitted for publication in international peer-reviewed journals and the key findings will be presented at international scientific conferences.
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